Data / Medical devices / Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) / United States
FDA-registered makers of Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) in the United States: 20 establishments
20 establishments in the United States are registered with the FDA to make Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) (product code DWL). 11 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
- Product code
- DWL
- Country
- United States
Makers of Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| BSN medical Inc. | Charlotte, NC, United States | Complaint file establishment, Specification developer | 3 | August 20, 1999 | 0 | 0 | 0 | api.fda.gov |
| 3M Company | Saint Paul, MN, United States | Complaint file establishment, Specification developer | 2 | December 20, 2012 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 2 | August 21, 2014 | 0 | 0 | 0 | api.fda.gov |
| Barton-Carey Medical Products, Inc. | Jellico, TN, United States | Manufacturer | 1 | February 13, 1986 | 0 | 0 | 0 | api.fda.gov |
| Bossong Hosiery Mills | Asheboro, NC, United States | Manufacturer | 1 | April 2, 2013 | 0 | 0 | 0 | api.fda.gov |
| BSN medical inc. | Hickory, NC, United States | Manufacturer | 1 | April 4, 1994 | 0 | 0 | 0 | api.fda.gov |
| Djo, LLC | Carlsbad, CA, United States | Specification developer | 1 | December 6, 1993 | 0 | 0 | 0 | api.fda.gov |
| Elastic Therapy, LLC | Asheboro, NC, United States | Contract manufacturer, Manufacturer | 1 | December 6, 1993 | 0 | 0 | 0 | api.fda.gov |
| Gottfried Medical, Inc. | Toledo, OH, United States | Manufacturer | 1 | January 12, 1983 | 0 | 0 | 0 | api.fda.gov |
| Surgical Appliance Industries, Inc. | Cincinnati, OH, United States | Contract manufacturer, Manufacturer, Repackager or relabeler | 1 | April 27, 2012 | 0 | 0 | 0 | api.fda.gov |
| Thuasne, LLC | Hamlet, NC, United States | Contract manufacturer, Manufacturer | 1 | July 24, 2009 | 0 | 0 | 0 | api.fda.gov |
| Carolon Co. | Rural Hall, NC, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Encompass Group, LLC. | McDonough, GA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ideavillage Products Corp. | Wayne, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medi MFG., Inc. | Whitsett, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medi Usa, LP | Whitsett, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Runway Knitting Inc | Rainsville, AL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sleeve Stars LLC | Estero, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STS Corporation | Duluth, GA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.